My hubby applied for pip he has fybromyalgia I amthe parky person, he submited his claim in april last year and only recieved his first payment in january, and that was only after i rang them a couple of times it seemed to take forever.
I have been waiting for an assessment for 4 months I believe I will be assessed by atos
I rang a welfare rights helpline number and was told some people have been waiting over 12 months
my response to that was so some people will die while waiting for PIP.
Its an absolute disgrace in a country like the UK but in a drive to save money the government has targeted the wrong people
The other thing I would say is why would I personally need to be independently assessed as I have a condition PD thats going to get regretfully worse its not like I have caught a cold or am making out I have some mystery illness. I mean why don't they just write to my GP and the Walton centre they should be able to tell them all they need to know.
Why I will tell you why because by dragging you down the interview road if you don't give them all the information or make a mistake in what you say which can happen to anyone they wont allow your claim and theres another few bob saved
Thanks for reading and I do wish you all success...............Paul
hope it all works out,i know its to easy to get a sick note of your gp,but if they cant take the word of a neurologist its wrong.If they did it this way it would save whole lot of money.
I do sympathise with you i originally started my pip claim in September 2013 , i only had my home assessment on 6th March 2014 , hopefully i am now in the final stages of the application my reports are apparently with the decision maker at DWP
I had to get my MP involved and also given my story to the journalists to get where i am today with my pip claim it has been a complete from the start .
Good luck with the claim Paul i recommend talking to your MP .
I did what Shelly said and went through my MP I have a pip assessment tomorrow thanks to you all for all your help I would advise anyone on this board with PD to use your MP they are your representative they are there to help you at the end of the day its a genuine claim for PIP its a regretful debilitating condition you have'nt caught a cold.
Bit nervous about the assessment Shelly what are they like hope they dont shout or try to over bear
So glad things worked out and you have your assessment at last
They ask you about a typical day what problems you have doing everyday things , if you have any aids or appliances that you use tell them about them and also if a aid or appliance would help you if you had one , you dont have to have them to score the points as long as they would help you , you score the points
Have posted a link to help you
Not overbearing at all my assessor was really nice , although they will make informal observations, ie my assessor noted i had severe tremors when passing him my medication and that i also spilt a drink over me due to tremors